Trisodium 5-amino-4-hydroxy-3-[(4-sulphonatophenyl)azo]naphthalene-2,7-disulphonate

Base Information

Chemical Name:Trisodium 5-amino-4-hydroxy-3-[(4-sulphonatophenyl)azo]naphthalene-2,7-disulphonate
CAS No.:17716-41-5
Molecular Formula:C₁₆H₁₀N₃O₁₀S₃*3Na
Molecular Weight:569.437
Hs Code.:
European Community (EC) Number:241-718-6
ChEMBL ID:CHEMBL1269836
Mol file:17716-41-5.mol

Synonyms:CHEMBL1269836;5-amino-4-hydroxy-3-[(4-sulfophenyl)diazenyl]naphthalene-2,7-disulfonic acid;Trisodium 5-amino-4-hydroxy-3-[(4-sulphonatophenyl)azo]naphthalene-2,7-disulphonate;17716-41-5;SCHEMBL7065494;BDBM50328753;5-amino-4-hydroxy-3-((4-sulfonatophenyl)diazenyl)naphthalene-2,7-disulfonate

Suppliers and Price of Trisodium 5-amino-4-hydroxy-3-[(4-sulphonatophenyl)azo]naphthalene-2,7-disulphonate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 5 raw suppliers

Chemical Property of Trisodium 5-amino-4-hydroxy-3-[(4-sulphonatophenyl)azo]naphthalene-2,7-disulphonate

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:g/cm³
XLogP3:0.7
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:13
Rotatable Bond Count:5
Exact Mass:502.97630714
Heavy Atom Count:32
Complexity:1020

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC(=CC=C1N=NC2=C(C3=C(C=C(C=C3C=C2S(=O)(=O)O)S(=O)(=O)O)N)O)S(=O)(=O)O

Technology Process of Trisodium 5-amino-4-hydroxy-3-[(4-sulphonatophenyl)azo]naphthalene-2,7-disulphonate

There total 3 articles about Trisodium 5-amino-4-hydroxy-3-[(4-sulphonatophenyl)azo]naphthalene-2,7-disulphonate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 5460-09-3
1-amino-8-hydroxy-naphthalene-3,6-disulphonic acid monosodium salt

: 4-(2-chlorodiazenyl)benzenesulfonic acid

: 17716-41-5,36105-98-3
C₁₆H₁₀N₃O₁₀S₃^(3-)*3Na⁽¹⁺⁾

Guidance literature:: With sodium carbonate; In water; N,N-dimethyl-formamide; for 28.1667h; pH=9 - 10;
DOI:10.1016/j.saa.2013.05.089

Reference yield:

: 17716-41-5,36105-98-3
C₁₆H₁₀N₃O₁₀S₃^(3-)*3Na⁽¹⁺⁾

Guidance literature:: With hydrogenchloride; In water; N,N-dimethyl-formamide; at 25 ℃;

With sodium nitrite; In water; N,N-dimethyl-formamide;

In water; N,N-dimethyl-formamide; at 25 ℃; for 0.00833333h;

Reference yield:

: 90-20-0
4-amino-5-hydroxy-2,7-naphthalenedisulfonic acid

: 121-57-3,856062-06-1
4-aminobenzene sulfonic acid

: 17716-41-5,36105-98-3
C₁₆H₉N₃O₁₀S₃^(4-)*4Na⁽¹⁺⁾

Guidance literature:: With hydrogenchloride; aminosulfonic acid; sodium hydrogencarbonate; sodium nitrite; Multistep reaction; 1) H₂O, 5 min;
DOI:10.1021/ac00241a049